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Results:
1-10
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Results: 10
Authors:
Scott, HS
Kudoh, J
Wattenhofer, M
Shibuya, K
Berry, A
Chrast, R
Guipponi, M
Wang, J
Kawasaki, K
Asakawa, S
Minoshima, S
Younus, F
Mehdi, SQ
Radhakrishna, U
Papasavvas, MP
Gehrig, C
Rossier, C
Korostishevsky, M
Gal, A
Shimizu, N
Bonne-Tamir, B
Antonarakis, SE
Citation: Hs. Scott et al., Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness, NAT GENET, 27(1), 2001, pp. 59-63
Authors:
Radhakrishna, U
Senol, S
Herken, H
Gucuyener, K
Gehrig, C
Blouin, JL
Akarsu, NA
Antonarakis, SE
Citation: U. Radhakrishna et al., An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree, EUR J HUM G, 9(1), 2001, pp. 39-44
Authors:
Ben-Yosef, T
Wattenhofer, M
Riazuddin, S
Ahmed, ZM
Scot, HS
Kudoh, J
Shibuya, K
Antonarakis, SE
Bonne-Tamir, B
Radhakrishna, U
Naz, S
Ahmed, Z
Riazuddin, S
Pandya, A
Nance, WE
Wilcox, ER
Friedman, TB
Morell, RJ
Citation: T. Ben-yosef et al., Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness, J MED GENET, 38(6), 2001, pp. 396-400
Authors:
Quintana-Murci, L
Krausz, C
Zerjal, T
Sayar, SH
Hammer, MF
Mehdi, SQ
Ayub, Q
Qamar, R
Mohyuddin, A
Radhakrishna, U
Jobling, MA
Tyler-Smith, C
McElreavey, K
Citation: L. Quintana-murci et al., Y-chromosome lineages trace diffusion of people and languages in southwestern Asia, AM J HU GEN, 68(2), 2001, pp. 537-542
Authors:
Lamartine, J
Essenfelder, GM
Kibar, Z
Lanneluc, I
Callouet, E
Laoudj, D
Lemaitre, G
Hand, C
Hayflick, SJ
Zonana, J
Antonarakis, S
Radhakrishna, U
Kelsell, DP
Christianson, AL
Pitaval, A
Der Kaloustian, V
Fraser, C
Blanchet-Bardon, C
Rouleau, GA
Waksman, G
Citation: J. Lamartine et al., Mutations in GJB6 cause hidrotic ectodermal dysplasia, NAT GENET, 26(2), 2000, pp. 142-144
Authors:
Kibar, Z
Dube, MP
Powell, J
McCuaig, C
Hayflick, SJ
Zonana, J
Hovnanian, A
Radhakrishna, U
Antonarakis, SE
Benohanian, A
Sheeran, AD
Stephan, ML
Gosselin, R
Kelsell, DP
Christianson, AL
Fraser, FC
Kaloustian, VMD
Rouleau, GA
Citation: Z. Kibar et al., Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping, EUR J HUM G, 8(5), 2000, pp. 372-380
Authors:
Blouin, JL
Meeks, M
Radhakrishna, U
Sainsbury, A
Gehring, C
Sail, GD
Bartoloni, L
Dombi, V
O'Rawe, A
Walne, A
Chung, E
Afzelius, BA
Armengot, M
Jorissen, M
Schidlow, DV
van Maldergem, L
Walt, H
Gardiner, RM
Probst, D
Guerne, PA
Delozier-Blanchet, CD
Antonarakis, SE
Citation: Jl. Blouin et al., Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity, EUR J HUM G, 8(2), 2000, pp. 109-118
Authors:
Antonarakis, SE
Blouin, JL
Lasseter, VK
Gehrig, C
Radhakrishna, U
Nestadt, G
Housman, DE
Kazazian, HH
Kalman, K
Gutman, G
Fantino, E
Chandy, KG
Gargus, JJ
Arm, E
Citation: Se. Antonarakis et al., Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21, AM J MED G, 88(4), 1999, pp. 348-351
Authors:
Curtis, L
Blouin, JL
Radhakrishna, U
Gehrig, C
Lasseter, VK
Wolyniec, P
Nestadt, G
Dombroski, B
Kazazian, HH
Pulver, AE
Housman, D
Bertrand, D
Antonarakis, SE
Citation: L. Curtis et al., No evidence for linkage between schizophrenia and markers at chromosome 15q13-14, AM J MED G, 88(2), 1999, pp. 109-112
Authors:
Radhakrishna, U
Bornholdt, D
Scott, HS
Patel, UC
Rossier, C
Engel, H
Bottani, A
Chandal, D
Blouin, JL
Solanki, JV
Grzeschik, KH
Antonarakis, SE
Citation: U. Radhakrishna et al., The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations, AM J HU GEN, 65(3), 1999, pp. 645-655
Risultati:
1-10
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